RIVA, PAOLA VANDA
RIVA, PAOLA VANDA
Dipartimento di Biotecnologie Mediche e Medicina Traslazionale
19p deletion in recurring leiomyosarcoma lesions from the same patient
2000-06-01 P. Riva, L. Dalprá, V. Gualandri, M. Volontè, M. Miozzo, R. Malgara, A. F. Conti, L. Larizza
1p36 LOH and expression study of apoptotic genes in a selected group of chordomas
2006-01-01 M. Longoni, F. Orzan, M. Stroppi, N. Boari, P. Mortini, P. Riva
The 3' untranslated region of human cyclin-dependent kinase 5 regulatory subunit 1 contains regulatory elements affecting transcript stability
2007-12-03 S. Moncini, A. Bevilacqua, M. Venturin, C. Fallini, A. Ratti, A. Nicolin, P. Riva
A 12-bp deletion (7818del12) in the c-kit protooncogene in a large Italian kindred with piebaldism
1995-01-01 P. Riva, N. Milani, P. Gandolfi, L. Larizza
A novel potentially diagnostic polymorphism (4894 A/C) in exon 10 of the human c-kit proto-oncogene
1996-10-01 P. Riva, L. Larizza
A tandem duplication of chromosome 21 in a newborn showing a phenotype inconsistent with Down syndrome
2010-04-01 E. Martinoli, G.V. Zuccotti, L. Pogliani, M. Volontè, M. Venturin, P. Fortina, A. Ertel, S. Redaelli, P.V. Riva, L. Dalprà
ADAP2 in heart development: a candidate gene for the occurrence of cardiovascular malformations in NF1 microdeletion syndrome
2014-01-01 M. Venturin, S. Carra, G. Gaudenzi, S. Brunelli, G.R. Gallo, S. Moncini, F. Cotelli, P. Riva
Breakpoint characterization of a novel NF1 multiexonic deletion : a case showing expression of the mutated allele
2008-05-01 F. Orzan, M. Stroppi, M. Venturin, M.C. Valero, C. Hernández, P. Riva
Centaurin-α2 Interacts with β-Tubulin and Stabilizes Microtubules
2012-12-01 P. Zuccotti, D. Cartelli, M. Stroppi, V. Pandini, M. Venturin, A. Aliverti, E. Battaglioli, G. Cappelletti, P.V. Riva
Characterization of a cytogenetic 17q11.2 deletion in an NF1 patient with a contiguous gene syndrome
1996-12-01 P. Riva, P. Castorina, S. Manoukian, L. Dalprà, L. Doneda, G. Marini, J. den Dunnen, L. Larizza
Characterization of a non-recurrent familial translocation t(7;9)(q11.23;p24.3) points to a recurrent involvement of the Williams-Beuren syndrome region in chromosomal rearrangements
2006-01-01 G. Portera, M. Venturin, A. Patrizi, E. Martinoli, P. Riva, L. Dalprà
Chromosomal instability in Cancer : a genomic condition reflecting alterations of different cellular mechanisms
2008-01-01 P. Riva, M. Longoni
Chromosomal instability in fibroblasts and mesenchymal tumors from 2 sibs with Rothmund-Thomson syndrome
1998-08-12 M. Miozzo, P. Castorina, P. Riva, L. Dalprà, A. M. Fuhrman Conti, L. Volpi, T. S. Hoe, A. Khoo, J. Wiegant, C. Rosenberg, L. Larizza
Cromosomi umani
2013-01-01 P.V. Riva
Current therapeutic options and novel molecular markers in skull base chordomas
2012-01-01 F. Gagliardi, N. Boari, P. Riva, P. Mortini
Developmental abnormalities and cancer predisposition in neurofibromatosis type 1
2009-01-01 L. Larizza, C.C.G. Gervasini, F. Natacci, P.V. Riva
Differential allelic expression of SOS1 and hyperexpression of the activating SOS1 c.755C variant in a Noonan syndrome family
2015-01-01 S. Moncini, M.T. Bonati, I. Morella, L. Ferrari, R. Brambilla, P. Riva
Differential allelic expression of the SOS1 c.755C activating variant in a Noonan syndrome family
2014-05-01 S. Moncini, M.T. Bonati, I. Morella, L. Ferrari, R. Brambilla, P. Riva
Digenic inheritance of subclinical variants in Noonan Syndrome patients: an alternative pathogenic model?
2020-06-01 L. Ferrari, E. Mangano, M.T. Bonati, I. Monterosso, D. Capitanio, F. Chiappori, I. Brambilla, C. Gelfi, C. Battaglia, R. Bordoni, P. Riva
The discovery of a new role of HDAC8 in skeletal muscle differentiation and in centronuclear myopathy insurgence
2018-06-17 L. Ferrari, C. Bragato, L. Brioschi, S. Esposito, M. Mazzola, A. Pezzotta, F. Pizzetti, A. Moreno-Fortuny, P. Riva, F. Frabetti, P. Viani, G. Cossu, M. Mora, A. Marozzi, A. Pistocchi